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. 2019 Aug 13;10(4):e01698-19. doi: 10.1128/mBio.01698-19

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Relevant genotype and/or characteristic(s) Reference or source
P. aeruginosa strains used
in the infectiona
    PA14-1 Barcode CAAAAGGACA; Gent
    PAO1-B11 Barcode GTGTCGTGGG; Gent
    B23-2 Wound isolate; barcode GCCTATTGTG; Gent Lubbock, TX
    CF18-1 Nonmucoid CF isolate; barcode GTTACGTCAA; Gent 60
    MSH10-2 Water isolate; barcode TATCAGATTT; Gent 60
    S54485-1 UTIb isolate; barcode TTAAACTAGG; Gent 60
P. aeruginosa strains
    PA14
    PA14ΔwspF Clean wspF deletion
    PAO1
    PAO1ΔwspF Clean wspF deletion (JJH356)
    PA14-1attB::lacZ lacZ from miniCTX-lacZ introduced at the attB site This study
    RSCV-2 wt-wspA Variant wspA replaced by the wild-type allele This study
    RSCV-1 wt-wspA Variant wspA replaced by the wild-type allele This study
    RSCV-40 wt-wspA Variant wspA replaced by the wild-type allele This study
E. coli strains
    NEB5-α NEBc
    S17 NEB
Plasmids
    pEX18Ap Gene deletion vector 47
    pEX18Ap::wt-wspA wspA-complementing construct This study
    pCdrA::gfp CdrA promoter fused to gfp; Carb 31
    pMH487 Empty vector for pCdrA::gfp; Carb 31
    pJN2133 PA2133 cloned into pJN105; Gent 32
    pHERD20T Empty vector; Carb 56
    pHERD2133 PA2133 from pJN2133 cloned into pHEDR20T; Carb This study
    miniCTX-lacZ Tet 58
a

All strains used in the infection are resistant to gentamicin. Barcodes are located at the Tn7 site on the genome.

b

UTI, urinary tract infection.

c

NEB, New England Biolabs.